Reaction
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Type (Example)
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Pyrazoles
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N-Methyl substituted using Mono methyl hydrazine
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Suzuki Coupling Reactions
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Substituted Biphenyls
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Chiral Chemistry
|
Chiral transformations
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Acylation
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Friedel-Craft, Houben-Hoesch, Vilsmeier-Haak Fries rearrangement
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Reduction
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Beechamp reduction, Hydrogenation, Clemmensen and Hydride
|
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Darzen's Reaction
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Glycidic ester
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Diazotisation
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Anilines
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Halogenation
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Photochlorination,Bromination, Chlorination
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Nitration
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Aromatic Compounds
|
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Olefin Formation
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Wittig
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Phosphorylation
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Organo phosphorous & sulfur compounds
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Sandmeyer Reaction
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Synthetic intermediates
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Thionation
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Organo phosphorous & sulfur compounds
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Rearrangement
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Thermal Cyclisation
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Multi Phase Reactions
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Phase-transfer catalysis
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Alkylation
|
C, O & N alkylation
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Esterification
|
Phenols & carboxylic acid esters
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Organometallic
|
Grignard, Wittig
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High Temperature Reactions
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Up to 260º C
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High Pressure Reactions
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Up to 25 bars
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Acetylation
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Alcohols and Phenols
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Cyanation
|
Cyano hydrins from Aldehydes and Ketones
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Pyridines
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Substituted derivatives
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PI continously adds to its reaction capabilities in order to meet customer requirements.
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